Postoperative Pain Management in Rhinoplasty: A Double Blind Randomized Controlled Trial

dc.contributor.authorKandathil, Cherian Kurian
dc.contributor.authorSpataro, Emily A.
dc.contributor.authorSaltychev, Mikhail
dc.contributor.authorKalebjian, Roushig
dc.contributor.authorPatel, Priyesh N.
dc.contributor.authorKim, Cherine H.
dc.contributor.authorAkkina, Sarah R.
dc.contributor.authorKimura, Kyle S.
dc.contributor.authorRossi-Meyer, Monica
dc.contributor.authorLongino, Elizabeth S.
dc.contributor.authorTruong, Henry
dc.contributor.authorMost, Sam P.
dc.contributor.organizationfi=fysiatria|en=Physical and Rehabilitation Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.17712075286
dc.converis.publication-id516139624
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/516139624
dc.date.accessioned2026-05-04T20:12:17Z
dc.description.abstract<h3>Background:</h3><p>There is inadequate evidence for the utilization of nonnarcotic pain medications for postoperative pain management following rhinoplasty.</p><h3>Objective:</h3><p>To compare the effectiveness of opioid and non-opioid medications for postoperative pain control in rhinoplasty as measured by a visual analog scale (VAS) on postoperative days 0–5.</p><h3>Methods:</h3><p>In this double-blind randomized controlled clinical trial, adult patients who underwent primary rhinoplasty at a tertiary center were enrolled from August 2019 to October 2024. Patients were randomized to receive either a combination of acetaminophen (325 mg) and hydrocodone (5 mg) or acetaminophen (325 mg) and ibuprofen (200 mg), 1–2 tablets every 4 h for five postoperative days. Tramadol (50 mg) was prescribed for breakthrough pain.</p><h3>Results:</h3><p>A total of 130 patients (65 per group) completed the study. The average age (SD) was 32 (10.7) years. The majority were women (77%), White (68%), and underwent combined functional and aesthetic rhinoplasty (52%). There was no difference detected in mean postoperative pain (VAS) scores recorded on postoperative days 0–5, between treatment groups (<em>p</em> = 0.156). Among side effects, only itchiness was significantly higher (<em>p</em> = 0.001) in the hydrocodone–acetaminophen group.</p><h3>Conclusion:</h3><p>This trial demonstrates a lack of difference between opioid and non-opioid pain medications in postoperative pain control after rhinoplasty.</p>
dc.identifier.eissn2689-3622
dc.identifier.jour-issn2689-3614
dc.identifier.urihttps://www.utupub.fi/handle/11111/60293
dc.identifier.urlhttps://doi.org/10.1177/26893614261429310
dc.identifier.urnURN:NBN:fi-fe2026050438227
dc.language.isoen
dc.okm.affiliatedauthorSaltychev, Mikhail
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMary Ann Liebert
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumber26893614261429310
dc.relation.doi10.1177/26893614261429310
dc.relation.ispartofjournalFacial Plastic Surgery & Aesthetic Medicine
dc.titlePostoperative Pain Management in Rhinoplasty: A Double Blind Randomized Controlled Trial
dc.year.issued2026

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